Suppr超能文献

TLPLDC疫苗作为III/IV期黑色素瘤手术切除后辅助治疗的IIb期随机对照试验:初步分析

A Phase IIb Randomized Controlled Trial of the TLPLDC Vaccine as Adjuvant Therapy After Surgical Resection of Stage III/IV Melanoma: A Primary Analysis.

作者信息

Vreeland Timothy J, Clifton Guy T, Hale Diane F, Chick Robert C, Hickerson Annelies T, Cindass Jessica L, Adams Alexandra M, Bohan Phillip M Kemp, Andtbacka Robert H I, Berger Adam C, Jakub James W, Sussman Jeffrey J, Terando Alicia M, Wagner Thomas, Peoples George E, Faries Mark B

机构信息

Department of Surgery, Uniformed Services University of Health Sciences, Bethesda, MD, USA.

Department of Surgical Oncology, Brooke Army Medical Center, San Antonio, TX, USA.

出版信息

Ann Surg Oncol. 2021 Oct;28(11):6126-6137. doi: 10.1245/s10434-021-09709-1. Epub 2021 Feb 27.

Abstract

BACKGROUND

Melanoma therapy has changed dramatically over the last decade with improvements in immunotherapy, yet many patients do not respond to current therapies. This novel vaccine strategy may prime a patient's immune system against their tumor and work synergistically with immunotherapy against advanced-stage melanoma.

METHODS

This was a prospective, randomized, double-blind, placebo-controlled, phase IIb trial of the tumor lysate, particle-loaded, dendritic cell (TLPLDC) vaccine administered to prevent recurrence in patients with resected stage III/IV melanoma. Patients were enrolled and randomized 2:1 to the TLPLDC vaccine or placebo (empty yeast cell wall particles and autologous dendritic cells). Both intention-to-treat (ITT) and per treatment (PT) analyses were predefined, with PT analysis including patients who remained disease-free through the primary vaccine/placebo series (6 months).

RESULTS

A total of 144 patients were randomized (103 vaccine, 41 control). Therapy was well-tolerated with similar toxicity between treatment arms; one patient in each group experienced related serious adverse events. While disease-free survival (DFS) was not different between groups in ITT analysis, in PT analysis the vaccine group showed improved 24-month DFS (62.9% vs. 34.8%, p = 0.041).

CONCLUSIONS

This phase IIb trial of TLPLDC vaccine administered to patients with resected stage III/IV melanoma shows TLPLDC is well-tolerated and improves DFS in patients who complete the primary vaccine series. This suggests patients who do not recur early benefit from TLPLDC in preventing future recurrence from melanoma. A phase III trial of TLPLDC + checkpoint inhibitor versus checkpoint inhibitor alone in patients with advanced, surgically resected melanoma is under development.

TRIAL REGISTRATION

NCT02301611.

摘要

背景

在过去十年中,随着免疫疗法的改进,黑色素瘤治疗发生了巨大变化,但许多患者对当前疗法没有反应。这种新型疫苗策略可能会激发患者的免疫系统对抗肿瘤,并与针对晚期黑色素瘤的免疫疗法协同作用。

方法

这是一项前瞻性、随机、双盲、安慰剂对照的IIb期试验,对肿瘤裂解物负载颗粒的树突状细胞(TLPLDC)疫苗进行研究,用于预防III/IV期黑色素瘤切除患者的复发。患者按2:1随机分组接受TLPLDC疫苗或安慰剂(空酵母细胞壁颗粒和自体树突状细胞)。预先定义了意向性治疗(ITT)和 per treatment(PT)分析,PT分析包括在初级疫苗/安慰剂系列(6个月)中保持无病的患者。

结果

共有144名患者被随机分组(103名疫苗组,41名对照组)。治疗耐受性良好,各治疗组之间毒性相似;每组各有一名患者发生相关严重不良事件。虽然ITT分析中各治疗组间无病生存期(DFS)无差异,但在PT分析中,疫苗组的24个月DFS有所改善(62.9%对34.8%,p = 0.041)。

结论

这项针对III/IV期黑色素瘤切除患者的TLPLDC疫苗IIb期试验表明,TLPLDC耐受性良好,可改善完成初级疫苗系列患者的DFS。这表明未早期复发的患者可从TLPLDC预防黑色素瘤未来复发中获益。一项针对晚期手术切除黑色素瘤患者的TLPLDC + 检查点抑制剂与单纯检查点抑制剂的III期试验正在开展。

试验注册

NCT02301611

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48d9/7914039/e7b4e9a8b0e3/10434_2021_9709_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验